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      <dc:title>Zinc-doped iron oxide nanoparticles as a proton-activatable agent for dose range verification in proton therapy</dc:title>
      <dc:creator>España Palomares, Samuel</dc:creator>
      <dc:creator>Espinosa Rodríguez, Andrea</dc:creator>
      <dc:creator>Garcia Diez, Miguel</dc:creator>
      <dc:creator>Martinez Nouvilas, Victor</dc:creator>
      <dc:creator>Sánchez Tembleque Verbo, Víctor</dc:creator>
      <dc:creator>Udías Moinelo, José Manuel</dc:creator>
      <dc:creator>Valladolid Onecha, Víctor</dc:creator>
      <dc:creator>Fraile Prieto, Luis Mario</dc:creator>
      <dc:description>Artículo firmado por 23 autores</dc:description>
      <dc:description>Proton therapy allows the treatment of specific areas and avoids the surrounding tissues. However, this technique has uncertainties in terms of the distal dose fall-off. A promising approach to studying the proton range is the use of nanoparticles as proton-activatable agents that produce detectable signals. For this, we developed an iron oxide nanoparticle doped with Zn (IONP@Zn-cit) with a hydrodynamic size of 10 nm and stability in serum. Cytotoxicity, defined as half of the surveillance, was 100 μg Zn/mL in the U251 cell line. The effect on clonogenic cell death was tested after X-ray irradiation, which suggested a radioprotective effect of these nanoparticles at low concentrations (1–10 μg Zn/mL). To evaluate the production of positron emitters and prompt-gamma signals, IONP@Zn-cit was irradiated with protons, obtaining prompt-gamma signals at the lowest measured concentration (10 mg Zn/mL). Finally, 67Ga-IONP@Zn-cit showed accumulation in the liver and spleen and an accumulation in the tumor tissue of 0.95% ID/g in a mouse model of U251 cells. These results suggest the possibility of using Zn nanoparticles as proton-activatable agents to verify the range by prompt gamma detection and face the challenges of prompt gamma detection in a specific biological situation, opening different avenues to go forward in this field.</dc:description>
      <dc:date>2024-03-14T16:13:35Z</dc:date>
      <dc:date>2024-03-14T16:13:35Z</dc:date>
      <dc:date>2023-09-29</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>Ibáñez-Moragues, M., Fernández-Barahona, I., Santacruz, R., Oteo, M., Luján-Rodríguez, V. M., Muñoz-Hernando, M., ... &amp; Morcillo, M. Á. (2023). Zinc-Doped Iron Oxide Nanoparticles as a Proton-Activatable Agent for Dose Range Verification in Proton Therapy. Molecules, 28(19), 6874.</dc:identifier>
      <dc:identifier>10.3390/molecules28196874</dc:identifier>
      <dc:identifier>https://hdl.handle.net/20.500.14352/102235</dc:identifier>
      <dc:identifier>1420-3049</dc:identifier>
      <dc:identifier>https://www.mdpi.com/1420-3049/28/19/6874</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>B2017/BMD-3888 PRONTO-CM</dc:relation>
      <dc:relation>S2022/BMD-7434 ASAP-CM</dc:relation>
      <dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-104558RB-I00/ES/RADIOBIOLOGIA EN LA TERAPIA DE PROTONES. BASES PARA LA COMBINACION DE LA TERAPIA DE PROTONES E INMUNOTERAPIA/</dc:relation>
      <dc:relation>TED2021-130592B-I00</dc:relation>
      <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
      <dc:rights>open access</dc:rights>
      <dc:rights>Attribution 4.0 International</dc:rights>
      <dc:publisher>MDPI</dc:publisher>
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